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Sumitomo Pharma Senior Clinical Trial Associate, Oncology in Dover, Delaware

Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed products in the U.S., Canada, and Europe, a diverse pipeline of early- to late-stage assets, and in-house advanced technology capabilities, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website https://www.us.sumitomo-pharma.com (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=3440496098&u=https%3A%2F%2Fwww.us.sumitomo-pharma.com%2F&a=https%3A%2F%2Fwww.us.sumitomo-pharma.com+) or follow us on LinkedIn (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=2504638834&u=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsumitomo-pharma-america%2F&a=LinkedIn) .

Job Overview

The Sr. Clinical Trial Associate (CTA) is responsible for supporting the conduct of clinical trials and handling administrative aspects of clinical trial execution. This role will support completion of all study deliverables, ensuring the highest level of data quality; proactively identifies, communicates, and resolves clinical study operational issues; and participates in process improvement initiatives as required.

Job Duties and Responsibilities

Leads completion of general administrative tasks to support team members with clinical trial execution, e.g., development and formatting of documents, review and reconciliation of study- specific information, etc.
Maintains study status updates on a weekly basis (e.g., IRB approvals, regulatory document collection, patient enrollment, monitoring status, etc.) or as defined by project team
Tracks, prepares and reports study-specific information using databases, spreadsheets, and other tools
Drafts, reviews and in some cases approves study documents, including essential document packets, study plans/manuals, templates, informed consent forms, etc.
Manages clinical and non-clinical supplies, including purchase and shipping, if needed
Develops and distributes electronic site file documents
Schedules/coordinates meetings, takes and distributes meeting minutes
Supports protocol and study-specific training with vendors, site personnel, and clinical sites
Coordinates laboratory sample shipments between clinical sites and central laboratories and tracking the status of samples and resulting laboratory data
Collaborates with the Clinical Regulatory Operations Specialist to support overall quality, maintenance, and completeness of Trial Master Files
May assume certain trial management activities to support the study lead and the project team
Acts as a mentor to more junior Clinical Trial Associates
Performs other duties as assigned

Key Core Competencies

Knowledge of global regulatory and compliance requirements for clinical research
Knowledge and experience with Trial Master Files (TMF) and experience with electronic TMF systems (i.e., Veeva)
Ability to work in a fast-paced environment with demonstrated ability to manage multiple competing tasks and demands.
Excellent communication and interpersonal skills are essential as the CTA interacts with many people of varying levels of responsibility for clinical trial programs
Ability to collaborate effectively with internal and external study management teams to meet project timelines
Ability to prioritize and complete tasks according to deadline.
Problem solving study-related issues; demonstrating resourcefulness, independence and appropriate escalation of issues as needed
Excellent writing skills to assist with creation of file notes, team communications, and other documents as assigned.
Strong computer skills in MS Office including (Word, Excel, PowerPoint), MS Project, Smartsheet, and other applicable applications.

Education and Experience

Bachelor’s degree or equivalent curriculum (scientific or healthcare discipline preferred)
A minimum of 2 years of relevant experience is preferred

The base salary range for this role is $82,600 to $103,200. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes unlimited paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law.

Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.

Confidential Data : All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential.

Compliance :Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards.

Mental/Physical Requirements : Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.

Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer

Sumitomo Pharma America (SMPA) is committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

For more information about EEO and the Law, please visit the following pages:

Equal Employment Opportunity is THE LAW (https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf)

EEO is the Law Poster Supplement

Pay Transparency (https://www.dol.gov/sites/dolgov/files/OFCCP/pdf/pay-transp_%20English_formattedESQA508c.pdf)

At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company’s cultural pillars.

Our Mission

To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people worldwide

Our Vision

For Longer and Healthier Lives, we unlock the future with cutting edge technology and ideas

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Sumitomo Pharma Senior Clinical Trial Associate, Oncology in Dover, Delaware

Sumitomo Pharma

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